Reprise Biomedical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Reprise Biomedical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Miro3D Fibers Wound Matrix, MiroDry Wound Matrix, MiroTract Wound Matrix
4
Total
4
Cleared
0
Denied
Reprise Biomedical, Inc. has 4 FDA 510(k) cleared medical devices. Based in Plymouth, US.
Latest FDA clearance: Apr 2024. Active since 2022. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Reprise Biomedical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by DuVal & Associates, P.A. as regulatory consultant.
FDA 510(k) Regulatory Record - Reprise Biomedical, Inc.
4 devices